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Microglia are a type of glial cell located throughout the brain and spinal cord of the central nervous system (CNS). [1] Microglia account for about 10–15% of cells found within the brain. [2] As the resident macrophage cells, they act as the first and main form of active immune defense in the CNS. [3]
He managed to identify microglia between 1919 and 1921 by staining the cells with silver carbonate. [3] His method of staining also led to the discovery of oligodendroglia in 1921, [4] which both he and Penfield are now credited with. [2] However it was Rio Hortega who named the cells. [1]
CD163 (Cluster of Differentiation 163) is a protein that in humans is encoded by the CD163 gene. [5] CD163 is the high affinity scavenger receptor for the hemoglobin-haptoglobin complex [6] and in the absence of haptoglobin - with lower affinity - for hemoglobin alone. [7]
Immunofluorescence staining of homeostatic microglia in a healthy adult mouse retina. Microglia are the tissue-resident phagocytes of the central nervous system . CSF1R signaling promotes migration of primitive microglia precursor cells from the embryonic yolk sac to the developing brain prior to formation of the blood-brain-barrier .
ED1 is the most widely used monoclonal antibody clone directed against the rat CD68 protein and is used to identify macrophages, Kupffer cells, osteoclasts, monocytes, and activated microglia in rat tissues. [13] [14] [15] In this species, it is expressed in most macrophage populations and thus ED1 is commonly used as a pan-macrophage marker. [16]
When microglia interact with the deposited fibrillar forms of β-amyloid it leads to the conversion of the microglia into an activated cell and results in the synthesis and secretion of cytokines and other proteins that are neurotoxic. [2] One preliminary model as to how this would occur involves a positive feedback loop.
Immunoperoxidase is a type of immunostain used in molecular biology, medical research, and clinical diagnostics.In particular, immunoperoxidase reactions refer to a sub-class of immunohistochemical or immunocytochemical procedures in which the antibodies are visualized via a peroxidase-catalyzed reaction.
In microscopy, negative staining is an established method, often used in diagnostic microscopy, for contrasting a thin specimen with an optically opaque fluid. In this technique, the background is stained, leaving the actual specimen untouched, and thus visible. This contrasts with positive staining, in which the actual specimen is stained.